Canonical Allele Identifier: CA2014278166

Gene: GNB3 CDCA3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6845470C= , CM000674.2:g.6845470C=	GRCh38
NC_000012.11:g.6954634C= , CM000674.1:g.6954634C=	GRCh37
NC_000012.10:g.6824895C=	NCBI36
NG_009100.1:g.10260C=
NG_009100.2:g.10260C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229264.8:c.700-116C= (GNB3) MANE Select	ENSP00000229264.3:n.700-116C=
ENST00000229264.7:c.700-116C= (GNB3)	ENSP00000229264.3:n.700-116C=
ENST00000422785.7:c.*1318G= (CDCA3)	ENSP00000415142.2:n.*1318G=
ENST00000435982.6:c.697-116C= (GNB3)	ENSP00000414734.2:n.697-116C=
ENST00000537035.1:c.577-116C= (GNB3)	ENSP00000445967.1:n.577-116C=
ENST00000540458.5:n.2051-116C= (GNB3)
ENST00000542751.1:n.104C= (GNB3)
ENST00000603043.1:n.1384G= (CDCA3)
ENST00000604599.1:n.2246G= (CDCA3)
NM_001297571.1:c.697-116C= (GNB3)	NP_001284500.1:n.697-116C=
NM_002075.3:c.700-116C= (GNB3)	NP_002066.1:n.700-116C=
XM_011520953.1:c.700-116C= (GNB3)	XP_011519255.1:n.700-116C=
XM_011520954.1:c.697-116C= (GNB3)	XP_011519256.1:n.697-116C=
XM_011521027.1:c.*2059G= (CDCA3)	XP_011519329.1:n.*2059G=
XM_011521028.1:c.*2059G= (CDCA3)	XP_011519330.1:n.*2059G=
XM_011521029.1:c.*2277G= (CDCA3)	XP_011519331.1:n.*2277G=
XM_011521030.1:c.*2210G= (CDCA3)	XP_011519332.1:n.*2210G=
XM_011520953.3:c.700-116C= (GNB3)	XP_011519255.1:n.700-116C=
XR_001748879.2:n.3604G= (CDCA3)
XR_001748880.2:n.2955G= (CDCA3)
XR_001748881.2:n.2864G= (CDCA3)
XR_002957383.1:n.3106G= (CDCA3)
XR_002957384.1:n.4017G= (CDCA3)
XR_002957385.1:n.3497G= (CDCA3)
NM_001297571.2:c.697-116C= (GNB3)	NP_001284500.1:n.697-116C=
NM_002075.4:c.700-116C= (GNB3) MANE Select	NP_002066.1:n.700-116C=
NM_001297603.3:c.*1318G= (CDCA3)	NP_001284532.1:n.*1318G=